510(k) K942629
K942629 is an FDA 510(k) premarket notification submitted by National Custom Ent., Inc. for the device "NCE REPLACEMENT BATTERIES". The FDA issued a decision of Substantially Equivalent on August 18, 1994. The device falls under product code DPS (Electrocardiograph), a Class II device regulated under 21 CFR 870.2340. National Custom Ent., Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 18, 1994
- Date Received
- June 3, 1994
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Electrocardiograph
- Device Class
- Class II
- Regulation Number
- 870.2340
- Review Panel
- CV
- Submission Type